pre-update Archives

Press Coverage

通过人工智能推进生命科学的数据发现

Vyasa has developed deep-learning artificial intelligence solutions for organizations looking to solve the complex data…

Certara2023 年 3 月 2 日

Video

Vyasa 演示

Certara2023 年 3 月 2 日

Press Release

Certara Announces Transition Plan For Chief Financial Officer

PRINCETON, N.J. – 2023 年 3 月 1 日 – Certara, Inc. （纳斯达克股票代码：CERT), announced today that John…

Certara2023 年 3 月 1 日

On-Demand Webinar

了解如何通过 PK 提交在几分钟内创建 CDISC domains

Creating CDISC domains as part of the pharmacokinetic (PK) deliverable for regulatory submissions can be…

Certara2023 年 3 月 1 日

White Paper

解读欧洲新临床试验法规（EU-CTR）

While the new EU-CTR will help to streamline clinical trials, which will benefit both patients…

Certara2023 年 2 月 27 日

Blog

Common Clinical Trial Disclosure Challenges & Potential Solutions

Pharmaceutical companies are being required to be more transparent through the timely disclosure of more…

Certara2023 年 2 月 24 日

网络研讨会点播

FDA Modernization Act 2.0 — 它对药品开发人员意味着什么？

历史上，FDA 要求药物发现与开发项目必须包含动物试验。This…

Certara2023 年 2 月 21 日

On-Demand Webinar

RAPS Sponsored: How Drug Developers Can Navigate the Inflation Reduction Act

The Inflation Reduction Act (enacted in August 2022) contains profound changes for the healthcare and…

Certara2023 年 2 月 10 日

On-Demand Webinar

Data Visualization with SEND Data to See What Happened at the Preclinical Phase

SEND is an implementation of CDISC’s (Clinical Data Interchange Standards Consortium) SDTM (Study Data Tabulation…

Certara2023 年 2 月 9 日

White Paper

A Guide to the UK Regulation of Medicines and Medical Devices Post-Brexit

Certara2023 年 2 月 8 日

pre-update

通过人工智能推进生命科学的数据发现

Vyasa 演示

Certara Announces Transition Plan For Chief Financial Officer

了解如何通过 PK 提交在几分钟内创建 CDISC domains

解读欧洲新临床试验法规（EU-CTR）

Common Clinical Trial Disclosure Challenges & Potential Solutions

FDA Modernization Act 2.0 — 它对药品开发人员意味着什么？

RAPS Sponsored: How Drug Developers Can Navigate the Inflation Reduction Act

Data Visualization with SEND Data to See What Happened at the Preclinical Phase

A Guide to the UK Regulation of Medicines and Medical Devices Post-Brexit

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